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C8ORF44 抗体 (AA 81-159) (Biotin)

This anti-C8ORF44 antibody is a 兔 多克隆 antibody detecting C8ORF44 in WB, ELISA, IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN1699939
发货至: 中国

Quick Overview for C8ORF44 抗体 (AA 81-159) (Biotin) (ABIN1699939)

抗原

C8ORF44 (Chromosome 8 Open Reading Frame 44 (C8ORF44))

适用

宿主

  • 24

克隆类型

  • 24
多克隆

标记

  • 5
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This C8ORF44 antibody is conjugated to Biotin

应用范围

  • 18
  • 13
  • 13
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
    • 2
    • 1
    • 1
    • 1
    AA 81-159

    预测反应

    Human

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C8orf44

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    C8ORF44 (Chromosome 8 Open Reading Frame 44 (C8ORF44))

    别名

    C8orf44

    背景

    Synonyms: C8orf44, CH044_HUMAN, FLJ11267, Putative uncharacterized protein C8orf44.

    Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf44 gene product has been provisionally designated C8orf44 pending further characterization.

    基因ID

    56260
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